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rs137853322

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137853322(A;G)
Make rs137853322(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154564420
GeneIKBKG
is asnp
is mentioned by
dbSNPrs137853322
ebirs137853322
HLIrs137853322
Exacrs137853322
Varsomers137853322
Maprs137853322
PheGenIrs137853322
hapmaprs137853322
1000 genomesrs137853322
hgdprs137853322
ensemblrs137853322
gopubmedrs137853322
geneviewrs137853322
scholarrs137853322
googlers137853322
pharmgkbrs137853322
gwascentralrs137853322
openSNPrs137853322
23andMers137853322
23andMe allrs137853322
SNP Nexus

SNPshotrs137853322
SNPdbers137853322
MSV3drs137853322
GWAS Ctlgrs137853322
Max Magnitude0
OMIM300248
Desc
Variant0005
Relatedalso
ClinVar
Risk rs137853322(G;G)
Alt rs137853322(G;G)
Reference rs137853322(A;A)
Significance Pathogenic
Disease Incontinentia pigmenti syndrome
Variation info
Gene IKBKG
CLNDBN Incontinentia pigmenti syndrome
Reversed 0
HGVS NC_000023.10:g.153792635A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000012202.3,